Home LiteratureArticle Details
PMID: 1518064 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cell-cycle control of a cloned chromosomal origin of replication from Caulobacter crescentus.

Journal of molecular biology ·Vol. 226 ·No. 4 ·1992-08-20 ·Pages 959-77

Marczynski GT, Shapiro L

Abstract

Caulobacter crescentus cell division is asymmetric and yields distinct swarmer cell and stalked cell progeny. Only the stalked cell initiates chromosomal replication, and the swarmer cell must differentiate into a stalked cell before chromosomal DNA replication can occur. In an effort to understand this developmental control of replication, we employed pulsed-field gel electrophoresis to localize and to isolate the chromosomal origin of replication. The C. crescentus homologues of several Escherichia coli genes are adjacent to the origin in the physical order hemE, origin, dnaA and dnaK,J. Deletion analysis reveals that the minimal sequence requirement for autonomous replication is greater than 430 base-pairs, but less than 720 base-pairs. A plasmid, whose replication relies only on DNA from the C. crescentus origin of replication, has a distinct temporal pattern of DNA synthesis that resembles that of the bona fide C. crescentus chromosome. This implies that cis-acting replication control elements are closely linked to this origin of replication. This DNA contains sequence motifs that are common to other bacterial origins, such as five DnaA boxes, an E. coli-like 13-mer, and an exceptional A + T-rich region. Point mutations in one of the DnaA boxes abolish replication in C. crescentus. This origin also possesses three additional motifs that are unique to the C. crescentus origin of replication: seven 8-mer (GGCCTTCC) motifs, nine 8-mer (AAGCCCGG) motifs, and five 9-mer (GTTAA-n7-TTAA) motifs are present. The latter two motifs are implicated in essential C. crescentus replication functions, because they are contained within specific deletions that abolish replication.

Related Genes
MeSH Terms
Bacterial Proteins/genetics Caulobacter crescentus/metabolism Cell Cycle/physiology Cell Differentiation/physiology Chromosome Mapping Chromosomes, Bacterial Cloning, Molecular DNA Mutational Analysis DNA Replication DNA, Bacterial/isolation & purification DNA-Binding Proteins/genetics Escherichia coli Proteins Genes, Bacterial/genetics HSP40 Heat-Shock Proteins HSP70 Heat-Shock Proteins Heat-Shock Proteins/genetics Plasmids/genetics Regulatory Sequences, Nucleic Acid/genetics
Chemicals
Bacterial Proteins DNA, Bacterial DNA-Binding Proteins DnaA protein, Bacteria Escherichia coli Proteins HSP40 Heat-Shock Proteins HSP70 Heat-Shock Proteins Heat-Shock Proteins dnaK protein, E coli
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Marczynski G T
Department of Developmental Biology, Beckman Center, Stanford University School of Medicine, CA 94305.
Shapiro L
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
1992-08-20
Pages
959-77
Language
English
Region
England
NLM ID
2985088R
Subset
IM
Grants
NIGMS NIH HHS · GM32506 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]